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This document explains: how patients are tested and treated, and steps in place to prevent its spread.
Export controls applying to Weapons of Mass Destruction (WMD) related activities - transfer of technology and provision of technical support
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
The civil procedure rules govern the way civil cases are managed, and set out the processes of the Civil Division of the Court of Appeal, the High Court and the County Court.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Check how much your visa application costs in the country you’re in
A CV is a summary of your skills, achievements and experience that you use to apply for jobs. Check advice on what to include and how to make it stand out.
Find out who can get a free rapid lateral flow test, how to use the test and what your test result means.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Student visa - check which courses you can study, prepare supporting documents, apply, what happens at the UK border
Advice for medical professionals to follow when assessing drivers with neurological disorders.
The Multidisciplinary University Research Initiative (MURI) is a US Department of Defense (DoD) programme.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
The characteristics, diagnosis, management, surveillance and epidemiology of Klebsiella species.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
Volume 23 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
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